| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44966316-44966566 | Common:1; Rare:100 | ||||
| chr20:45363346-45363550 | Common:2; Rare:53 | ||||
| chr20:45416013-45416207 | Rare:71; Clinvar:1 | ||||
| chr20:45469684-45469900 | Rare:83 | ||||
| chr20:45791870-45792007 | Common:1; Rare:51 | ||||
| chr20:45812296-45812694 | Common:4; Rare:117 | ||||
| chr20:45857299-45857661 | Common:4; Rare:108 | ||||
| chr20:45881053-45881254 | Common:2; Rare:50 | ||||
| chr20:45891227-45891379 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45911661-45911691 | Rare:6 | ||||
| chr20:45912141-45912279 | Common:3; Rare:32 | ||||
| chr20:45934627-45934731 | Rare:54 | ||||
| chr20:46021602-46021746 | Common:3; Rare:37 | ||||
| chr20:46089841-46090083 | Rare:80 | ||||
| chr20:46363975-46364049 | Common:1; Rare:14 |